视网膜骨厚度作为梅尼埃病发育不良内型的放射学标志。

Amy F Juliano, Kuei-You Lin, Nitesh Shekhrajka, Donghoon Shin, Steven D Rauch, Andreas H Eckhard
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引用次数: 0

摘要

背景和目的:梅尼埃病(MD)有两种主要的内型:一种是内淋巴囊发育不全、发育不良(MD-hp),另一种是内淋巴囊发育正常,但随着时间的推移会发生退化(MD-dg)。确定患者的具体内淋巴型对于预测疾病进展、为患者量身定制咨询方案和优化治疗策略非常重要。内型诊断包括测量前庭导水管的角度轨迹(ATVA),ATVA≥140°表示MD-hp,ATVA≤120°表示MD-dg。本研究旨在探讨 ATVA 与迷走神经后骨厚度之间的联系,以此作为一种替代诊断方法,利用 CT 和 MR 成像区分 MD 内型:对 32 名确诊 MD 的成年患者(60 耳)和 33 名无 MD 或其他内耳症状的年龄匹配对照者(61 耳)的 CT颞骨成像进行了回顾性审查。在标准化轴向 CT 图像上采用统一方法测量 ATVA 和迷走神经后骨厚度。进行比较分析以确定 ATVA 和迷宫后骨厚度之间的相关性。此外,还对另外一组 11 名患者(22 耳)的颞骨 CT 和 MR 检查进行了回顾性复查,以测量迷宫后骨厚度,从而验证这两种检查方式之间的相关性:MD-hp(ATVA ≥140°)患者的平均迷走神经后骨厚度为 0.8 毫米(标度,0.3),MD-dg(ATVA ≤120°)患者的平均迷走神经后骨厚度为 2.0 毫米(标度,0.9)。在 MD 队列中进行的接收器操作特征曲线分析显示,迷走神经后骨厚度≥1.2 毫米可有效排除 MD-hp。迷宫后骨厚度的测量结果具有极佳的交互可靠性,CT 和 MR 测量结果之间的相关性接近完美:事实证明,迷走神经后骨质厚度是区分 MD 内型的一种有用而简单的替代标记物,尤其有助于排除 MD-hp。包括迷走神经后骨厚度的信息应被视为MD成像报告的常规部分。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Retrolabyrinthine Bone Thickness as a Radiologic Marker for the Hypoplastic Endotype in Menière Disease.

Background and purpose: Menière disease (MD) manifests in 2 major endotypes: one with a hypoplastic, underdeveloped endolymphatic sac (MD-hp) and the other with a normally developed sac that degenerates over time (MD-dg). Determining the specific endotype in patients is important for predicting disease progression, tailoring patient counseling, and optimizing treatment strategies. Endotype diagnosis involves measuring an angular trajectory of the vestibular aqueduct (ATVA), with an ATVA ≥140° indicative of MD-hp and an ATVA ≤120° of MD-dg. However, assessing the ATVA can be challenging. This study aimed to explore the link between ATVA and the thickness of the retrolabyrinthine bone as an alternative diagnostic measure that could provide differentiation between MD endotypes using CT and MR imaging.

Materials and methods: Retrospective review of CT temporal bone imaging from 32 adult patients with definite MD (60 ears) and 33 age-matched controls without MD or other inner ear symptoms (61 ears) was performed. The ATVA and retrolabyrinthine bone thickness were measured using uniform methodology on standardized axial CT images. Comparative analyses were performed to determine the correlation between ATVA and retrolabyrinthine bone thickness. Additionally, from a separate cohort of 11 patients (22 ears), CT and MR examinations of the temporal bone were retrospectively reviewed for retrolabyrinthine bone thickness measurements, to verify the correlation across the 2 modalities.

Results: The average retrolabyrinthine bone thickness was statistically significantly different between MD endotypes, being a mean of 0.8 (SD, 0.3) mm in patients with MD-hp (ATVA ≥140°) and 2.0 (SD, 0.9) mm in patients with MD-dg (ATVA ≤120°), with a consistent pattern of thin retrolabyrinthine bone in MD-hp and variable thickness in MD-dg. Receiver operating characteristic curve analysis within the MD cohort revealed that a retrolabyrinthine bone thickness ≥1.2 mm effectively rules out MD-hp. Excellent interrater reliability was noted for the retrolabyrinthine measurement, and there was near-perfect correlation between CT and MR measurements.

Conclusions: Retrolabyrinthine bone thickness proved to be a useful and straightforward alternative marker for distinguishing MD endotypes, being particularly useful for excluding MD-hp. Including information on retrolabyrinthine bone thickness should be considered a routine part of reporting in the context of MD imaging.

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